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Nature Genetics|November 3, 2019
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular diseaseDerek Klarin, Emma Busenkell, Renae Judy, et al.JCO Oncology Practice|June 16, 2021
SARS-CoV-2 Seropositivity and Seroconversion in Patients Undergoing Active Cancer-Directed TherapyLova Sun, Sanjna Surya, Noah G Goodman, et al.Circulation. Cardiovascular Genetics|January 30, 2015
Exome sequencing in suspected monogenic dyslipidemiasNathan O Stitziel, Gina M Peloso, Marianne Abifadel, et al.Nature Medicine|January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associationsJoseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.JAMA|March 8, 2017
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery DiseaseAmit V Khera, Hong-Hee Won, Gina M Peloso, et al.Nature Communications|December 29, 2022
Genomics and phenomics of body mass index reveals a complex disease networkJie Huang, Jennifer E Huffman, Yunfeng Huang, et al.Nature Genetics|April 27, 2007
A variant in CDKAL1 influences insulin response and risk of type 2 diabetesValgerdur Steinthorsdottir, Gudmar Thorleifsson, Inga Reynisdottir, et al.Nature|April 14, 2017
Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinityDanish Saleheen, Pradeep Natarajan, Irina M Armean, et al.The New England Journal of Medicine|August 8, 2022
Germline Mutations in CIDEB and Protection against Liver DiseaseNiek Verweij, Mary E Haas, Jonas B Nielsen, et al.Diabetes|January 10, 2013
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from IndiaRicha Saxena, Danish Saleheen, Latonya F Been, et al.Pageof 75